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miR-106B-25 Cluster expression: a comparative human and canine osteosarcoma study
BACKGROUND: Osteosarcoma (OS) is the most common primary malignant bone tumour in dogs and human beings, characterised by similar genetic and clinical features. With the aim to define similarities and differences in the biological aspects involved in OS progression, a comparative study was performed...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061892/ https://www.ncbi.nlm.nih.gov/pubmed/32201579 http://dx.doi.org/10.1136/vetreco-2019-000379 |
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author | Leonardi, Leonardo Benassi, Maria Serena Pollino, Serena Locaputo, Carmen Pazzaglia, Laura |
author_facet | Leonardi, Leonardo Benassi, Maria Serena Pollino, Serena Locaputo, Carmen Pazzaglia, Laura |
author_sort | Leonardi, Leonardo |
collection | PubMed |
description | BACKGROUND: Osteosarcoma (OS) is the most common primary malignant bone tumour in dogs and human beings, characterised by similar genetic and clinical features. With the aim to define similarities and differences in the biological aspects involved in OS progression, a comparative study was performed to create a model to improve patient outcome. METHODS: First, the expression of microRNAs (miRNAs) belonging to the cluster miR-106b-25 (miR-106b, miR-25 and miR-93-5p) in human and canine OS tissue was compared. RESULTS: miR-25 and miR-106b presented a variable expression not significantly different from the corresponding normal bone, while miR-93-5p expression was increased in all OS specimens, with higher levels in the canine subset compared with human. Accordingly, its target p21 presented a weaker and less homogeneous immunostaining distribution in the canine group. Given the high expression of miR-93-5p in all OS specimens, the functional response of human 143B and canine DAN OS cells to miRNA inhibition was evaluated. Although p21 expression increased after miR-93-5p inhibition both at mRNA and protein level, a more significant cell response in terms of proliferation and apoptosis was seen in canine OS cells. CONCLUSIONS: In conclusion, canine OS tissue and cell line presented higher expression levels of miR-93-5p than human OS. In addition, the introduction of miR-93-5p inhibitor caused a cell response in 143B and DAN that differed for the more intense functional impact in the canine OS cell line. |
format | Online Article Text |
id | pubmed-7061892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-70618922020-03-20 miR-106B-25 Cluster expression: a comparative human and canine osteosarcoma study Leonardi, Leonardo Benassi, Maria Serena Pollino, Serena Locaputo, Carmen Pazzaglia, Laura Vet Rec Open Companion or Pet Animals BACKGROUND: Osteosarcoma (OS) is the most common primary malignant bone tumour in dogs and human beings, characterised by similar genetic and clinical features. With the aim to define similarities and differences in the biological aspects involved in OS progression, a comparative study was performed to create a model to improve patient outcome. METHODS: First, the expression of microRNAs (miRNAs) belonging to the cluster miR-106b-25 (miR-106b, miR-25 and miR-93-5p) in human and canine OS tissue was compared. RESULTS: miR-25 and miR-106b presented a variable expression not significantly different from the corresponding normal bone, while miR-93-5p expression was increased in all OS specimens, with higher levels in the canine subset compared with human. Accordingly, its target p21 presented a weaker and less homogeneous immunostaining distribution in the canine group. Given the high expression of miR-93-5p in all OS specimens, the functional response of human 143B and canine DAN OS cells to miRNA inhibition was evaluated. Although p21 expression increased after miR-93-5p inhibition both at mRNA and protein level, a more significant cell response in terms of proliferation and apoptosis was seen in canine OS cells. CONCLUSIONS: In conclusion, canine OS tissue and cell line presented higher expression levels of miR-93-5p than human OS. In addition, the introduction of miR-93-5p inhibitor caused a cell response in 143B and DAN that differed for the more intense functional impact in the canine OS cell line. BMJ Publishing Group 2020-03-08 /pmc/articles/PMC7061892/ /pubmed/32201579 http://dx.doi.org/10.1136/vetreco-2019-000379 Text en © British Veterinary Association 2020. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, an indication of whether changes were made, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Companion or Pet Animals Leonardi, Leonardo Benassi, Maria Serena Pollino, Serena Locaputo, Carmen Pazzaglia, Laura miR-106B-25 Cluster expression: a comparative human and canine osteosarcoma study |
title | miR-106B-25 Cluster expression: a comparative human and canine osteosarcoma study |
title_full | miR-106B-25 Cluster expression: a comparative human and canine osteosarcoma study |
title_fullStr | miR-106B-25 Cluster expression: a comparative human and canine osteosarcoma study |
title_full_unstemmed | miR-106B-25 Cluster expression: a comparative human and canine osteosarcoma study |
title_short | miR-106B-25 Cluster expression: a comparative human and canine osteosarcoma study |
title_sort | mir-106b-25 cluster expression: a comparative human and canine osteosarcoma study |
topic | Companion or Pet Animals |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061892/ https://www.ncbi.nlm.nih.gov/pubmed/32201579 http://dx.doi.org/10.1136/vetreco-2019-000379 |
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